NOVY CORNUAL CANNULATION SET— 510(k) K931476

Clearance details

Applicant

Cook Ob/Gyn

Product code

Code MOV

Device class

Class 2

Regulation

21 CFR 884.4530

Advisory panel

Obstetrics/Gynecology

Date received

1993-03-24

Decision date

1995-07-28

Decision

Substantially Equivalent

Clearance type

Traditional

Location

Spencer, IN, US

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Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K931476.